Dubost Thoracic Retractor Blade 2605-4544

GUDID 00192896117242

Dubost Thoracic Retractor Large Blade Titanium

SONTEC INSTRUMENTS, INC.

Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable

• Primary Device ID: 00192896117242
• NIH Device Record Key: 9413aa5e-96c5-4319-ada0-57904b4a27ea
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dubost Thoracic Retractor Blade
• Version Model Number: 2605-4544
• Catalog Number: 2605-4544
• Company DUNS: 040729840
• Company Name: SONTEC INSTRUMENTS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896117242 [Primary]

FDA Product Code

• GAD: RETRACTOR

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00192896117242]

Dry Heat Sterilization

[00192896117242]

Dry Heat Sterilization

[00192896117242]

Dry Heat Sterilization

[00192896117242]

Dry Heat Sterilization

[00192896117242]

Dry Heat Sterilization

[00192896117242]

Dry Heat Sterilization

[00192896117242]

Dry Heat Sterilization

[00192896117242]

Dry Heat Sterilization

[00192896117242]

Dry Heat Sterilization

[00192896117242]

Dry Heat Sterilization

[00192896117242]

Dry Heat Sterilization

[00192896117242]

Dry Heat Sterilization

[00192896117242]

Dry Heat Sterilization

[00192896117242]

Dry Heat Sterilization

[00192896117242]

Dry Heat Sterilization

[00192896117242]

Dry Heat Sterilization

[00192896117242]

Dry Heat Sterilization

[00192896117242]

Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-04-09
• Device Publish Date: 2024-04-01

On-Brand Devices [Dubost Thoracic Retractor Blade]

• 00192896117242: Dubost Thoracic Retractor Large Blade Titanium
• 00192896117235: Dubost Thoracic Retractor Medium Blade Titanium
• 00192896117228: Dubost Thoracic Retractor Small Blade Titanium